Generation and comparative kinetic analysis of new glycosynthase mutants from streptococcus pyogenes fndoglycosidases for antibody glycoengineering

ABSTRACT

The present invention provides for recombinant Endo-S mutants (named Endo-S glycosynthases) that exhibit reduced hydrolysis activity and increased transglycosylation activity for the synthesis of glycoproteins wherein a desired sugar chain is added to a fucosylated or nonfucosylated GlcNAc-IgG acceptor. As such, the present invention allows for the synthesis and remodeling of therapeutic antibodies thereby providing for certain biological activities, such as, prolonged half-life time in vivo, less immunogenicity, enhanced in vivo activity, increased targeting ability, and/or ability to deliver a therapeutic agent.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to U.S. Provisional Application No. 62/526,635 filed on Jun. 29, 2017, the contents of which are incorporated by reference herein for all purposes.

GOVERNMENT RIGHTS IN INVENTION

This invention was made with government support under R01GM096973B and R01 GM080374 by the US National Institutes of Health. The government has certain rights in the invention.

BACKGROUND OF THE INVENTION Field of the Invention

The invention relates to glycoprotein synthesis, and more particularly, to the use of a recombinant and mutant Endo S, an Endo-β-N-acetylglucosaminidase from Streptococcus pyogenes, that possesses transglycosylation activity and limited hydrolyzing activity thereby providing for efficient glycosylation remodeling of antibody-Fc domain.

Description of the Related Art

Therapeutic monoclonal antibodies (mAbs) represent a rapidly expanding class of biologics that are widely used for the treatment of cancer, inflammation, and infectious diseases¹⁻³. Previous studies have shown that glycosylation affects a wide range of properties of antibodies, including structural integrity, serum half-life, effector functions and therapeutic efficacy⁴. For instance, a lack of core fucosylation on IgG Fc N-glycans at Asn-297 can significantly enhance antibody-dependent cellular cytotoxicity (ADCC), and the engineered antibody therapeutics with low fucose content showed substantially enhanced therapeutic efficacy over their fucosylated counterparts⁵⁻⁷. Moreover, a minor sialylated component of intravenous immunoglobulin (IVIG) has demonstrated anti-inflammatory effects in animal models⁸⁻¹⁰. Nevertheless, antibody preparations from natural resources or recombinant protein expression typically contain a heterogeneous mixture of glycan structures and are not usually optimized for structure-function studies or their therapeutic purposes^(11, 12). For example, only a small percentage of antibody therapeutics carries non-fucosylated N-glycoforms that are most effective for their functions as anti-cancer drugs^(13, 14). Monoclonal antibodies carrying homogeneous glycan structures become essential materials for studying antibody glycosylation and the therapeutic outcome of antibody-based drugs.

Tremendous efforts have been pursued to optimize antibody glycosylation through engineering of the glycosylation biosynthetic pathway in various host expression systems¹⁵⁻¹⁷. Nevertheless, complete control of the glycosylation profile by host expression engineering remains a challenge and the glycoforms that can be accessed this way are limited¹⁵⁻¹⁷. An alternative approach to circumvent the heterogeneity of antibody glycosylation is to perform in vitro chemoenzymatic glycan remodeling using an endoglycosidase-catalyzed deglycosylation and glycosynthase-catalyzed re-glycosylation protocol¹⁸⁻²¹. In this method, heterogeneous N-glycans of antibody are released by the wild-type endoglycosidase, leaving only the innermost GlcNAc or Fucα1,6GlcNAc residue intact on the antibody backbone. Then, the well-defined glycan structures can be re-attached to the GlcNAc- or Fucα1,6GlcNAc containing antibody by an endoglycosidase or an endo-glycosynthase mutant in a site-specific manner to produce antibody with homogeneous glycoforms. In 2012, two endo-glycosynthase mutants, D233A and D233Q, of an endoglycosidase from Streptococcus pyogenes (Endo-S) were created that were able to transfer complex type N-glycans to the deglycosylated rituximab, which represents the first endo-glycosynthases generated from the GH family 18 enzymes²⁰. This discovery has since opened a new avenue to access structurally well-defined antibody glycoforms for structural and functional studies²²⁻²⁶. The crystal structure of Endo-S has been also solved and provided some insight into its catalytic mechanism^(27, 28). More recently new endo-glycosynthases mutants with much broader substrate specificity were also generated from Endo-S2²⁹, an endoglycosidase from Streptococcus pyogenes serotype M49 (Endo-S2)³⁰. A recent study of a systematic mutagenesis on Endo-S2 has shown that the nature of the amino acid substituents at the critical Asp-184 residue has a significant impact on the transglycosylation and/or the residual hydrolysis activity²⁹. However, a systematic mutagenesis on prototype enzyme Endo-S at the critical Asp-233 site has not been reported and the mechanism behind the observed difference in catalysis by different mutants remains to be characterized.

In light of the above known activities of Endo S, it would be advantageous to provide a mutant Endo-S that exhibits transglycosylating activity with reduced hydrolyzing activity.

SUMMARY OF THE INVENTION

The present invention provides for recombinant Endo-S and selected mutants thereof that exhibit reduced hydrolysis activity and increased transglycosylation activity for the synthesis of IgG antibodies and Fc fragments thereof, wherein a desired sugar chain is added to a core fucosylated or nonfucosylated GlcNAc-IgG acceptor. As such, the present invention allows for the synthesis and remodeling of therapeutic antibodies and Fc fragments thereof to provide for certain biological activities, such as, prolonged half-life time in vivo, less immunogenicity, enhanced in vivo activity, increased targeting ability, and/or ability to deliver a therapeutic agent.

In one aspect, the present invention provides for transglycosylation activity of an endo-β-N-acetylglucosamindase of Streptococcus pyogenes (SEQ ID NO: 1) and mutants thereof, wherein the mutants have at least 95% homology thereto and exhibit transglycosylation activity on both core fucosylated and nonfucosylated GlcNAc-IgG acceptors, wherein the endoglycosidases enable the transfer of an oligosaccharide (in the form of an activated sugar oxazoline) en bloc to a fucosylated or nonfucosylated GlcNAc-IgG (or an Fc fragment thereof) to form a new glycoform of IgG (or an Fc fragment thereof).

In another aspect, the present invention provides for Endo-S mutants that show remarkably enhanced transglycosylation efficiency and diminished or abrogated product hydrolytic activity. Mutants preferably include site-specific mutations including a mutation at Asp-233 including in particular, D233C (SEQ ID NO: 5), D233E (SEQ ID NO: 6), D233G (SEQ ID NO: 7), D233M (SEQ ID NO: 2) and D233N (SEQ ID NO: 8) and mutants have at least 95% homology thereto that demonstrate transglycosylation activities. A preferred mutant is D233M (SEQ ID NO: 2) but not limited thereto.

In a further aspect, the present invention provides for a chemoenzymatic method for the preparation of a homogeneous core fucosylated or nonfucosylated glycoforms of IgG antibodies, comprising:

a. providing an acceptor selected from the group consisting of a core fucosylated GlcNAc-IgG, nonfucosylated GlcNAc-IgG or corresponding IgG-Fc fragments; and b. reacting the acceptor with a donor substrate including an activated oligosaccharide moiety, in the presence of Streptococcus pyogenes Endo-S Asp-233-Met mutant to transfer the activated oligosaccharide moiety to the acceptor and yield the homogeneous fucosylated or nonfucosylated glycoprotein.

In a still further aspect, the present invention provides a method for preparing a core-fucosylated IgG or IgG-Fc fragment having a predetermined oligosaccharide moiety, comprising:

a. providing a core-fucosylated IgG acceptor comprising an asparagine-linked core-fucosylated N-acetylglucosamine (GlcNAc) residue; and b. enzymatically reacting the core-fucosylated IgG acceptor with an activated oligosaccharide donor in the presence of Endoglycosidase-S D233M (SEQ ID NO: 2) mutant or mutants have at least 95% homology thereto, wherein the activated oligosaccharide donor carries an oligosaccharide moiety comprising a predetermined number and type of sugar residues, wherein the oligosaccharide moiety is covalently linked to the core-fucosylated IgG acceptor, thereby preparing the core-fucosylated IgG or IgG-Fc fragment having the predetermined oligosaccharide moiety.

In yet another aspect, the present invention provides for an activated oligosaccharide moiety, such as glycan or oligosaccharide oxazoline, glycosyl fluoride, glycosyl azide or an aryl glycoside, as a donor substrate for the synthesis of homogeneous core-fucosylated glycoproteins or nonfucosylated glycoproteins. Preferably the activated oligosaccharide moiety is an oligosaccharide oxazoline.

In a further aspect, the present invention relates to a chemoenzymatic method for the preparation of a homogeneous fucosylated or nonfucosylated monomer antibody or Fc fragment thereof, said method comprising:

a. providing an acceptor selected from core fucosylated or nonfucosylated GlcNAc-antibody or Fc fragment thereof; and b. reacting the acceptor with a donor substrate in the presence a Streptococcus pyogenes Endo-S Asp-233-Met mutant (SEQ ID NO: 2) or mutants have at least 95% homology thereto, wherein the donor substrate comprises a predetermined oligosaccharide component with a defined number and type of sugar residues and specific linkage types, thereby providing the homogeneous fucosylated or nonfucosylated monomer antibody or Fc fragment thereof. In one embodiment, a fucosylated GlcNAc containing protein is an alpha-1-6-fucosyl-GlcNAc-protein.

In another aspect, the present invention relates to a method of remodeling an antibody or Fc fragment thereof with an oligosaccharide having a predetermined oligosaccharide component with a defined number and type of sugar residues and with specific linkage types, the method comprising:

a. providing a core fucosylated antibody or Fc fragment thereof comprising Fc N-glycans; b. treating the core fucosylated antibody or Fc fragment with a hydrolyzing endo-enzyme to yield a Asn-linked GlcNAc moiety; and c. attaching the oligosaccharide to the Asn-linked GlcNAc moiety in the presence of an Endo-S mutant having an amino acid sequence consisting of SEQ ID NO: 2, thereby adding the predetermined oligosaccharide component.

In a further aspect, the present invention relates to a remodeling method of a core fucosylated or nonfucosylated IgG or IgG-Fc fragment with an oligosaccharide having a predetermined oligosaccharide component with a defined number and type of sugar residues and with specific linkage types, the method comprising:

-   -   providing a core fucosylated or nonfucosylated IgG or IgG-Fc         fragment obtained from natural or recombinant sources carrying         heterogeneous N-glycans;     -   treating the natural or recombinant IgG or IgG-Fc fragment with         an endo-enzyme (a wild type endoglycosidase or a mutant         endoglycosidase with efficient hydrolytic activity) to hydrolyze         the bond between the two GlcNAc residues positioned closest to         the peptide domain thereby forming a deglycosylated protein         carrying a core fucosylated or nonfucosylated GlcNAc-acceptor;         and     -   attaching the predetermined oligosaccharide component to the         GlcNAc-acceptor to reconstitute the natural beta-1,4-glycosidic         bond through transglycosylation with a Streptococcus pyogenes         Endo-S Asp-233 mutant having an amino acid sequence SEQ ID NO: 2         or mutants have at least 95% homology thereto, thereby adding         the predetermined the oligosaccharide component to remodel the         core fucosylated or nonfucosylated IgG or IgG-Fc fragment.

Applicable oligosaccharide oxazolines include, but not limited to, high-mannose type, hybrid type, sialoglycan oxazoline and complex type N-glycan, as well as their selectively modified derivatives such as those with specific tags. Preferably, di-, tri-, tetra-, penta-, hexyl-, hepta-, octyl-, nona-, deca-, or undeca-saccharide oxazolines are utilized as donor substrates for a highly efficient chemoenzymatic synthesis of homogeneous core fucosylated or nonfucosylated IgG antibodies and IgG-Fc fragments.

In yet another aspect, the present invention relates to a method to synthesize a modified antibody or fragment thereof, the method comprising;

-   -   providing a naturally existing IgG antibody, a recombinant         antibody or a Fc domain carrying Fc N-glycans as precursors;     -   Fc deglycosylating using an endoglycosidase such as a wild         Endo-S to deglycosylate the Fc domain to form a GlcNAc-acceptor;         wherein the GlcNAc-acceptor is positioned on the Fc region of         the antibody and the GlcNAc-acceptor is either core fucosylated         or nonfucosylated; and     -   transglycosylating the GlcNAc-acceptor in the naturally existing         IgG antibody, the recombinant antibody or the Fc domain with an         oligosaccharide oxazoline or a sialoglycan oxazoline having a         predetermined number of sugar residues under the catalysis of an         Endo-S mutant enzyme comprising SEQ ID NO: 2 or mutants have at         least 95% homology thereto form the modified antibody with the         predetermined number of sugar residues.

In yet another aspect, the present invention provides a method of remodeling an intravenous immunoglobulin (IVIG) exhibiting Fc-sialylated glycoforms, the method comprising:

a. providing an IVIG carrying Fc N-glycans; b. Fc deglycosylating the Fc N-glycans using an endoglycosidase including wild Endo-S to form GlcNAc-acceptors; wherein the GlcNAc-acceptors are positioned on the Fc region of the IVIG and the GlcNAc-acceptors are either fucosylated or nonfucosylated; and c. transglycosylating the GlcNAc-acceptors with a sialoglycan oxazoline having a predetermined number of sugar residues under the catalysis of a Endo-S mutant enzyme comprising SEQ ID NO: 2 or mutants have at least 95% homology thereto to form a sialylated IVIG.

Another aspect of the present invention provides for an IVIG preparation containing composition comprising at least 90% of homogeneous sialylated Fc glycoforms to increase anti-inflammatory activity, wherein the sialylated Fc glycoforms are synthesized using a Streptococcus pyogenes Endo-S Asp-233-Met mutant (SEQ ID NO: 2) in combination with a GlcNAc moiety positioned on the Fc region of a deglycosylated WIG and a sialoglycan oxazoline having a predetermined number of sugar residues.

In a still further aspect, the present invention relates to a method of synthesizing homogeneous core fucosylated or nonfucosylated IgG antibodies or IgG-Fc fragments, the method comprising:

a. providing a natural or recombinant IgG antibody or IgG-Fc fragment, wherein the recombinant IgG or IgG-Fc is produced from a typical protein expression system, including but not limited to yeast, insect, plant, and any mammalian expression system; b. removing the N-glycans by an enzyme selected from the group consisting of Endo-H, Endo-A, Endo-S, and/or Endo-F3 to form a core fucosylated or nonfucosylated GlcNAc-containing protein; c. providing a sugar oxazoline or sialoglycan oxazoline with a desired oligosaccharide component comprising a defined number and type of sugar residues in the chain; and d. enzymatically transglycosylating the fucosylated or nonfucosylated GlcNAc-containing protein with a sugar oxazoline having a desired number of sugar residues or sialoglycan oxazoline having a desired number of sugar and sialic acid residues with an endoglycosidase selected from the group consisting of a Streptococcus pyogenes Endo-S Asp-233 mutant having a sequence SEQ ID NO: 2 or mutants have at least 95% homology thereto, thereby forming a homogeneous core fucosylated or nonfucosylated IgG antibody or IgG-Fc fragment having an extension of desired number of sugar residues and/or sialic acid.

It is envisioned that the oligosaccharide oxazoline or sialoglycan oxazoline having a predetermined oligosaccharide component with a defined number and type of sugar residues may further comprises an additional moiety or tag including, a therapeutic agent or drug such as for treating cancer, HIV or other viruses, substances that activates receptors on the cell plasma membrane, agents that affects intracellular chemistry, agents that affects cellular physics, genes, gene analogs, RNA, RNA analogs, DNA, DNA analogs, amino acid sequences of surface receptors such as CCR5 or CD4, antigenic structure having affinity for a specific antibody; amino acid sequences of receptor ligands such as gp120, gp41 or gp160, receptor antagonists, receptor blockers, enzymes, enzyme substrates, enzyme inhibitors, enzyme modulators, therapeutic proteins, protein analogs, metabolites, metabolite analogs, oligonucleotides, oligonucleotide analogs, antigens, antigen analogs, antibodies or fragments thereof, antibody analogs, an antibody different from the modified antibody which is reactive to another receptor bacteria, viruses, inorganic ions, metal ions, metal clusters, polymers, fluorescent compounds and any combinations thereof.

As such, the present invention further provides a delivery device for delivering a drug or therapeutic agent having biological activity to treat a condition, the delivery device comprising: a remodeled IgG or IgG-Fc fragment having a predetermined sugar chain or sialoglycan and a therapeutic agent or drug attached to the terminal sugar residue or sialic acid.

The present invention envisions modifying monoclonal antibodies related to HIV including, but not limited to 17b, 48d, A32, C11, 2G12, F240, IgG1b12, 19e, X5, TNX-355 and F91, all of which are commercially available.

Further antibodies related to cancer or other diseases may also be remodeled for individual fit to certain receptors thereby increasing biological activity, the monoclonal antibodies may include, but are not limited to, cetuximab, rituximab, muromonab-CD3, abciximab, daclizumab, basiliximab, palivizumab, infliximab, trastuzumab, gemtuzumab ozogamicin, alemtuzumab, ibritumomab tiuxetan, adalimumab, omalizumab, tositumomab, I-131 tositumomab, efalizumab, bevacizumab, panitumumab, pertuzumab, natalizumab, etanercept, IGN101 (Aphton), volociximab (Biogen Idec and PDL BioPharm), Anti-CD80 mAb (Biogen Idec), Anti-CD23 mAb (Biogen Idel), CAT-3888 (Cambridge Antibody Technology), CDP-791 (Imclone), eraptuzumab (Immunomedics), MDX-010 (Medarex and BMS), MDX-060 (Medarex), MDX-070 (Medarex), matuzumab (Merck), CP-675,206 (Pfizer), CAL (Roche), SGN-30 (Seattle Genetics), zanolimumab (Serono and Genmab), adecatumumab (Sereno), oregovomab (United Therapeutics), nimotuzumab (YM Bioscience), ABT-874 (Abbott Laboratories), denosumab (Amgen), AM 108 (Amgen), AMG 714 (Amgen), fontolizumab (Biogen Idec and PDL BioPharm), daclizumab (Biogent Idec and PDL BioPharm), golimumab (Centocor and Schering-Plough), CNTO 1275 (Centocor), ocrelizumab (Genetech and Roche), HuMax-CD20 (Genmab), belimumab (HGS and GSK), epratuzumab (Immunomedics), MLN1202 (Millennium Pharmaceuticals), visilizumab (PDL BioPharm), tocilizumab (Roche), ocrerlizumab (Roche), certolizumab pegol (UCB, formerly Celltech), eculizumab (Alexion Pharmaceuticals), pexelizumab (Alexion Pharmaceuticals and Procter & Gamble), abciximab (Centocor), ranibizimumab (Genetech), mepolizumab (GSK), TNX-355 (Tanox), or MYO-029 (Wyeth).

A still further aspect of the invention relates to a method of remodeling an antibody which initially includes a heterogeneous sugar chain, the method comprising:

a. removing the heterogeneous sugar chain from the antibody with an endoglycosidase to leave a single fucosylated- or nonfucosylated-GlcNAc moiety attached to an original glycosylation site; and b. transferring a core oligosaccharide or sialoglycan oxazoline with at least one tag to the fucosylated- or -nonfucosylated GlcNAc moiety by an endoglycosidase catalyzed transglycosylation to yield a tagged antibody, wherein the endoglycosidase is selected from the group consisting of Endo-S mutant comprising SEQ ID NO: 2.

The tag moiety may include, but is not limited to, antigens, therapeutic drugs such as for cancer or HIV, toxins, fluorescent probes, biotin, PEG species, lipids, or nucleotides.

In another aspect, the present invention provides for a composition comprising a Streptococcus pyogenes Endo-S Asp-233 mutant (D233M) comprising amino acid sequence SEQ ID NO:2.

In yet another aspect, the present invention provides a substantially homogeneous preparation of core fucosylate or nonfucosylated antibody or Fc fragment thereof having a predetermined oligosaccharide moiety, wherein the substantially homogeneous preparation is produced by any of the aforementioned methods. Also provided are compositions comprising such homogeneous preparations.

In a still further aspect, the present invention provides for a method of treatment using a remodeled antibody having a desired glycosylation state and/or sialylated form in an amount sufficient to modulate biological activity in the treated subject.

Other aspects, features and embodiments of the invention will be more fully apparent from the ensuing disclosure and appended claims.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows a comparison of the transglycosylation efficiencies between Endo-S D233M (SEQ ID NO: 2) and the previously reported Endo-S D233Q (SEQ ID NO: 3) and Endo-S D233A (SEQ ID NO: 4) with SCT-Oxazoline. The data sets presented here are representative of three independent experiments.

FIG. 2 shows Michaelis-Menten plots of Endo-S mutants (D233M and D233A) for the substrates. a) for the donor substrate (glycan oxazoline SCT-Oxa); b) for the acceptor substrate (the deglycosylated rituximab). The data sets presented here are representative of three independent experiments.

FIG. 3 shows Michaelis-Menten plots of Endo-S2 mutants (D184M and D184A) for the substrates. a) for the donor substrate (sugar oxazoline SCT-Oxa); b) for the acceptor substrate (the deglycosylated rituximab). The data sets presented here are representative of three independent experiments.

DETAILED DESCRIPTION OF THE INVENTION

The present invention shows a systematic mutagenic analysis at the Asp-233 of Endo-S and the evaluation of their catalytic activities. It was found herein that substitution of the Asp-233 with the other 19 conical amino acids led to significantly distinct effects on the hydrolysis and transglycosylation activity of Endo-S, with the D233M mutant showing the highest overall catalytic efficiency, defined by the transglycosylation/hydrolysis ratio. Kinetic studies on the D233M mutant of Endo-S, as well as the previously identified glycosynthase mutant D184M of wild type Endo-S2 (SEQ ID NO: 11), indicated that the enhanced overall catalytic efficacy of the Asp-to-Met mutants for the glycosyl donor substrate was mainly due to a much higher turnover number (k_(cat)) over the corresponding D233A or D184A mutant, respectively. Further, the Asp-to-Met mutants from both enzymes demonstrated a significantly higher substrate affinity for the glycosyl acceptor substrate, the deglycosylated antibody, than their Asp-to-Ala counterparts. These findings provide a mechanistic explanation for the enhanced catalytic activity of Endo-S D233M mutants

The practice of the present invention will employ, unless otherwise indicated, conventional techniques of immunology, molecular biology, microbiology, cell biology and recombinant DNA, which are within the skill of the art. See, e.g., Sambrook, et al. MOLECULAR CLONING: A LABORATORY MANUAL, 2nd edition (1989); CURRENT PROTOCOLS IN MOLECULAR BIOLOGY (F. M. Ausubel, et al. eds., (1987)); the series METHODS IN ENZYMOLOGY (Academic Press, Inc.): PCR 2: A PRACTICAL APPROACH (M. J. MacPherson, B. D. Hames and G. R. Taylor eds. (1995)), Harlow and Lane, eds. (1988) ANTIBODIES, A LABORATORY MANUAL, and ANIMAL CELL CULTURE (R. I. Freshney, ed. (1987)).

It is understood that aspects of the present invention described herein include “consisting” and/or “consisting essentially of” aspects.

Definitions

As used in the specification herein, “a” or “an” may mean one or more. As used herein in the claim(s), when used in conjunction with the word “comprising”, the words “a” or “an” may mean one or more than one. As used herein “another” may mean at least a second or more.

As used herein, “biological activity” refers to pharmacodynamic and pharmacokinetic properties including, for example, molecular affinity or resultant biochemical or physiological effect, receptor affinity or resultant biochemical or physiological effect, non-receptor affinity or biochemical or physiological effect, efficacy, bioavailability, absorption, distribution, metabolism, or elimination.

As used herein, “sugar” refers to an oxidized or nonoxidized carbohydrate-containing molecule, including, but not limited to, a monosaccharide, disaccharide, trisaccharide, oligosaccharide, or polysaccharide, including, for example, N-acetylglucosamine, mannose, galactose, N-acetylneuraminic acid (sialic acid), glucose, fructose, fucose, sorbose, rhamnose, mannoheptulose, N-acetylgalactosamine, dihydroxyacetone, xylose, xylulose, arabinose, glyceraldehyde, sucrose, lactose, maltose, trehalose, cellobiose or any combination thereof of the L- or D-isomer. Sugar further refers to, such molecules produced naturally, recombinantly, synthetically, and/or semi-synthetically.

As used herein, “homogenous” refers to core fucosylated glycoproteins or nonfucosylated glycoproteins wherein the oligosaccharide component comprises at least 75%, more preferably at least 80%, at least 85% or at least 90%, and most preferably at least 95% of the same number and types of sugar residues.

As used herein, “protein” or “glycoprotein” is interchangeable with the terms peptide and glycopeptide.

As used herein, “homology” refers to amino acid sequence having substantial identity or similarity between two polypeptides and having at least 90%, and more preferably at least 95% similarity to a reference polypeptide. For polypeptides, the length of comparison to obtain the above-described percent homologies between sequences will generally be at least 25 amino acids, alternatively at least 50 amino acids, more likely at least 100 amino acids, and most likely 200 amino acids or more. Substantially identity or homologous polypeptides include additions, truncations, internal deletions or insertions, conservative and non-conservative substitutions, or other modifications located at positions of the amino acid sequence which do not destroy the function of the endoglycosidase. Those of skill in the art will recognize the numerous amino acids that can be modified or substituted with other chemically similar residues without substantially altering activity.

As used herein, “modulates” refers to an increase or decrease in “biological activity”, as defined above, when comparing to a glycosylation-engineered antibody of the present invention to a non-glycosylation-engineered antibody.

As used herein, “immunoglobulin molecule” or “antibodies,” refers to molecules that contain an antigen binding site which specifically binds an antigen or an Fc region that binds to cell receptors. Structurally, the simplest naturally occurring antibody (e.g., IgG) comprises four polypeptide chains, two heavy (H) chains and two light (L) chains inter-connected by disulfide bonds. The natural immunoglobulins represent a large family of molecules that include several types of molecules, such as IgD, IgG, IgA, IgM and IgE. The term also encompasses hybrid antibodies, or altered antibodies, and fragments thereof, including Fc fragment(s).

Antibodies can be fragmented using conventional techniques as described herein and the fragments screened for utility in the same manner as described for whole antibodies. A Fab fragment of an immunoglobulin molecule is a multimeric protein consisting of the portion of an immunoglobulin molecule containing the immunologically active portions of an immunoglobulin heavy chain and an immunoglobulin light chain covalently coupled together and capable of specifically combining with an antigen. Fab and Fc fragments can be prepared by proteolytic digestion of substantially intact immunoglobulin molecules with papain using methods that are well known in the art. However, a Fab or Fc fragment may also be prepared by expressing in a suitable host cell the desired portions of immunoglobulin heavy chain and immunoglobulin light chain using methods known in the art.

As used herein, with respect to antibodies, “substantially pure” means separated from those contaminants that accompany it in its natural state or those contaminants generated or used in the process of the obtaining the antibody. This term further includes the desired product having a single glycosylation state, whether or not this state includes glycosylation at a single site or multiple sites. Typically, the antibody is substantially pure when it constitutes at least 60%, by weight, of the antibody in the preparation. For example, the antibody in the preparation is at least about 75%, in certain embodiments at least about 80%, in certain embodiments at about 85%, in certain embodiments at least about 90%, in certain embodiments at least about 95%, and most preferably at least about 99%, by weight, of the desired antibody. A substantially pure antibody includes a naturally, recombinantly, or synthetically produced antibody.

As used herein, “therapeutically effective amount” refers to an amount that results in an improvement or remediation of the symptoms of the disease or condition.

Antigens useful for attachment as a tag to a modified core fucosylated or nonfucosylated glycoprotein of the present invention and more preferably an antibody or fragment thereof may be a foreign antigen, an endogenous antigen, fragments thereof, or variants having the same functional activity.

As used herein, “endogenous antigen” refers to a protein or part thereof that is naturally present in the recipient animal cell or tissue, such as a cellular protein, an immunoregulatory agent, or a therapeutic agent.

As used herein, “foreign antigen” refers to a protein or fragment thereof, which is foreign to the recipient animal cell or tissue including, but not limited to, a viral protein, a parasite protein, an immunoregulatory agent, or a therapeutic agent.

The foreign antigen may be a protein, an antigenic fragment or antigenic fragments thereof that originate from viral and parasitic pathogens.

Alternatively, the foreign antigen may be encoded by a synthetic gene and may be constructed using conventional recombinant DNA methods; the synthetic gene may express antigens or parts thereof that originate from viral and parasitic pathogens. These pathogens can be infectious in humans, domestic animals or wild animal hosts.

The foreign antigen can be any molecule that is expressed by any viral or parasitic pathogen prior to or during entry into, colonization of, or replication in their animal host.

The viral pathogens, from which the viral antigens are derived include, but are not limited to, Orthomyxoviruses, such as influenza virus (Taxonomy ID: 59771); Retroviruses, such as RSV, HTLV-1 (Taxonomy ID: 39015) and HTLV-II (Taxonomy ID: 11909); Herpes viruses, such as EBV (Taxonomy ID: 10295), CMV (Taxonomy ID: 10358) or herpes simplex virus (ATCC #: VR-1487); Lentiviruses, such as HIV-1 (Taxonomy ID: 12721) and HIV-2 Taxonomy ID: 11709); Rhabdoviruses, such as rabies; Picornoviruses, such as Poliovirus (Taxonomy ID: 12080); Poxviruses, such as vaccinia Taxonomy ID: 10245); Rotavirus Taxonomy ID: 10912); and Parvoviruses, such as adeno-associated virus 1 (Taxonomy ID: 85106).

Examples of viral antigens include, but are not limited to, the human immunodeficiency virus antigens Nef (National Institute of Allergy and Infectious Disease HIV Repository Cat. #183; GenBank accession # AF238278), Gag, Env (National Institute of Allergy and Infectious Disease HIV Repository Cat. #2433; GenBank accession # U39362), Tat (National Institute of Allergy and Infectious Disease HIV Repository Cat. #827; GenBank accession # M13137), Rev (National Institute of Allergy and Infectious Disease HIV Repository Cat. #2088; GenBank accession # L14572), Pol (National Institute of Allergy and Infectious Disease HIV Repository Cat. #238; GenBank accession # AJ237568) and T cell and B cell epitopes of gp120; the hepatitis B surface antigen (GenBank accession # AF043578); rotavirus antigens, such as VP4 (GenBank accession # AJ293721) and VP7 (GenBank accession # AY003871); influenza virus antigens, such as hemagglutinin (GenBank accession # AJ404627); nucleoprotein (GenBank accession # AJ289872); and herpes simplex virus antigens, such as thymidine kinase (GenBank accession # AB047378).

The bacterial pathogens, from which the bacterial antigens are derived, include but are not limited to, Mycobacterium spp., Helicobacter pylori, Salmonella spp., Shigella spp., E. coli, Rickettsia spp., Listeria spp., Legionella pneumoniae, Pseudomonas spp., Vibrio spp., and Borellia burgdorferi.

Examples of protective antigens of bacterial pathogens include the somatic antigens of enterotoxigenic E. coli, such as the CFA/I fimbrial antigen and the nontoxic B-subunit of the heat-labile toxin; pertactin of Bordetella pertussis, adenylate cyclase-hemolysin of B. pertussis, fragment C of tetanus toxin of Clostridium tetani, OspA of Borellia burgdorferi, protective paracrystalline-surface-layer proteins of Rickettsia prowazekii and Rickettsia typhi, the listeriolysin (also known as “Llo” and “Hly”) and/or the superoxide dismutase (also know as “SOD” and “p60”) of Listeria monocytogenes; the urease of Helicobacter pylori, and the receptor-binding domain of lethal toxin and/or the protective antigen of Bacillus anthrax.

Example of antigens from biological weapons or pathogens include, but are not limited to, smallpox, anthrax, tularemia, plague, listeria, brucellosis, hepatitis, vaccinia, mycobacteria, coxsackievirus, tuberculosis, malaria, erhlichosis and bacterial meningitis.

The parasitic pathogens, from which the parasitic antigens are derived, include but are not limited to, Plasmodium spp., such as Plasmodium falciparum (ATCC#: 30145); Trypanosome spp., such as Trypanosoma cruzi (ATCC#: 50797); Giardia spp., such as Giardia intestinalis (ATCC#: 30888D); Boophilus spp.; Babesia spp., such as Babesia microti (ATCC#: 30221); Entamoeba spp., such as Entamoeba histolytica (ATCC#: 30015); Eimeria spp., such as Eimeria maxima (ATCC#40357); Leishmania spp., (Taxonomy ID: 38568); Schistosome spp., such as Schistosoma mansoni (GenBank accession # AZ301495); Brugia spp., such as Brugia malayi (GenBank accession # BE352806); Fascida spp., such as Fasciola hepatica (GenBank accession # AF286903); Dirofilaria spp., such as Dirofilaria immitis (GenBank accession # AF008300); Wuchereria spp., such as Wuchereria bancrofti (GenBank accession # AF250996); and Onchocerca spp; such as Onchocerca volvulus (GenBank accession # BE588251).

Examples of parasite antigens include, but are not limited to, the pre-erythrocytic stage antigens of Plasmodium spp. such as the circumsporozoite antigen of P. falciparum (GenBank accession # M22982) P vivax (GenBank accession # M20670); the liver stage antigens of Plasmodium spp, such as the liver stage antigen 1 (as referred to as LSA-1; GenBank accession # AF086802); the merozoite stage antigens of Plasmodium spp; such as the merozoite surface antigen-1 (also referred to as MSA-1 or MSP-1; GenBank accession # AF199410); the surface antigens of Entamoeba histolytica, such as the galactose specific lectin (GenBank accession # M59850) or the serine rich Entamoeba histolytica protein; the surface proteins of Leishmania spp, such as 63 kDa glycoprotein (gp63) of Leishmania major (GenBank accession # Y00647 or the 46 kDa glycoprotein (gp46) of Leishmania major; paramyosin of Brugia malayi (GenBank accession # U77590; the triose-phosphate isomerase of Schistosoma mansoni (GenBank accession # W06781; the secreted globin-like protein of Trichostrongylus colubriformis (GenBank accession # M63263; the glutathione-S-transferases of Fasciola hepatica (GenBank accession # M77682; Schistosoma bovis (GenBank accession # M77682); S. japonicum (GenBank accession # U58012; and KLH of Schistosoma bovis and S. japonicum (Bashir, et al., supra).

Examples of tumor specific antigens include prostate specific antigen (PSA), TAG-72 and CEA; human tyrosinase (GenBank accession # M27160); tyrosinase-related protein (also referred to as TRP; GenBank accession # AJ132933); and tumor-specific peptide antigens.

Examples of transplant antigens include the CD3 molecule on T cells and histocompatibility antigens such as HLA A, HLA B, HLA C, HLA DR and HLA.

Examples of autoimmune antigens include IAS β chain, which is useful in therapeutic vaccines against autoimmune encephalomyelitis (GenBank accession # D88762); glatamic acid decarboxylase, which is useful in therapeutic vaccines against insulin-dependent type 1 diabetes (GenBank accession # NM013445); thyrotropin receptor (TSHr), which is useful in therapeutic vaccines against Grave's disease (GenBank accession # NM000369) and tyrosinase-related protein 1, which is useful in therapeutic vaccines against vitiligo (GenBank accession # NM000550).

HIV drugs that may be used in the construction of the tagged antibodies or fragments thereof include, but are not limited to antiviral agents such as nucleoside RT inhibitors, CCR5 inhibitors/antagonists, viral entry inhibitors and their functional analogs. Specifically, an antiviral agent may nucleoside RT inhibitors, such as Zidovudine (ZDV, AZT), Lamivudine (3TC), Stavudine (d4T), Didanosine (ddl), Zalcitabine (ddC), Abacavir (ABC), Emirivine (FTC), Tenofovir (TDF), Delaviradine (DLV), Efavirenz (EFV), Nevirapine (NVP), Saquinavir (SQV), Ritonavir (RTV), Indinavir (IDV), Nelfinavir (NFV), Amprenavir (APV), Lopinavir (LPV), Atazanavir, Combivir (ZDV/3TC), Kaletra (RTV/LPV), Trizivir (ZDV/3TC/ABC);

CCR5 inhibitors/antagonists, such as SCH-C, SCH-D, PRO 140, TAK 779, TAK-220, RANTES analogs, AK602, UK-427, 857, monoclonal antibodies; and viral entry inhibitors, such as Fuzeon (T-20) (enfuvirtide), NB-2, NB-64, T-649, T-1249, SCH-C, SCH-D, PRO 140, TAK 779, TAK-220, RANTES analogs, AK602, UK-427, 857; and functional analogs or equivalents thereof.

It is envisioned that many different core fucosylated glycoproteins and nonfucosylated glycoproteins can be modified according to the methods of the present invention or used as a therapeutic agent for conjugation to a terminal sugar including but not limited to, adrenocorticotropic hormone (ACTH); adrenocorticotropic hormone derivatives (e.g., ebiratide); angiotensin; angiotensin II; asparaginase; atrial natriuretic peptides; atrial sodium diuretic peptides; bacitracin; beta-endorphins; blood coagulation factors VII, VIII and IX; blood thymic factor (FTS); blood thymic factor derivatives; bombesin; bone morphogenic factor (BMP); bone morphogenic protein; bradykinin; caerulein; calcitonin gene related polypeptide (CGRP); calcitonins; CCK-8; cell growth factors (e.g., EGF; TGF-alpha; TGF-beta; PDGF; acidic FGF; basic FGF); cerulein; chemokines; cholecystokinin; cholecystokinin-8; cholecystokinin-pancreozymin (CCK-PZ); colistin; colony-stimulating factors (e.g. CSF; GC SF; GMC SF; MC SF); corticotropin-releasing factor (CRF); cytokines; desmopressin; dinorphin; dipeptide; dismutase; dynorphin; eledoi sin; endorphins; endothelin; endothelin-antagonistic peptides; endotherins; enkephalins; enkephalin derivatives; epidermal growth factor (EGF); erythropoietin (EPO); follicle-stimulating hormone (FSH); gallanin; gastric inhibitory polypeptide; gastrin-releasing polypeptide (GRP); gastrins; G-CSF; glucagon; glutathione peroxidase; glutathio-peroxidase; gonadotropins (e.g., human chorionic gonadotrophin and .alpha. and .beta. subunits thereof); gramicidin; gramicidines; growth factor (EGF); growth hormone-releasing factor (GRF); growth hormones; hormone releasing hormone (LHRH); human artrial natriuretic polypeptide (h-ANP); human placental lactogen; insulin; insulin-like growth factors (IGF-I; IGF-II); interferon; interferons (e.g., alpha- beta- and gamma-interferons); interleukins (e.g. 1; 2; 3; 4; 5; 6; 7; 8; 9; 10; 11 and 12); intestinal polypeptide (VIP); kallikrein; kyotorphin; luliberin; luteinizing hormone (LH); luteinizing hormone-releasing hormone (LH-RH); lysozyme chloride; melanocyte-stimulating hormone (MSH); melanophore stimulating hormone; mellitin; motilin; muramyl; muramyldipeptide; nerve growth factor (NGF); nerve nutrition factors (e.g. NT-3; NT-4; CNTF; GDNF; BDNF); neuropeptide Y; neurotensin; oxytocin; pancreastatin; pancreatic polypeptide; pancreozymin; parathyroid hormone (PTH); pentagastrin; polypeptide YY; pituitary adenyl cyclase-activating polypeptides (PACAPs); platelet-derived growth factor; polymixin B; prolactin; protein synthesis stimulating polypeptide; PTH-related protein; relaxin; renin; secretin; serum thymic factor; somatomedins; somatostatins derivatives; superoxide dismutase; taftsin; tetragastrin; thrombopoietin (TPO); thymic humoral factor (THF); thymopoietin; thymosin; thymostimulin; thyroid hormone releasing hormone; thyroid-stimulating hormone (TSH); thyrotropin releasing hormone TRH); trypsin; tuftsin; tumor growth factor (TGF-alpha); tumor necrosis factor (TNF); tyrocidin; urogastrone; urokinase; vasoactive intestinal polypeptide; and vasopressin.

Core fucosylated and nonfucosylated glycoproteins are important classes of biomolecules that play crucial roles in many biological events such as cell adhesion, tumor metastasis, pathogen infection, and immune response. As indicated previously herein, a major problem in structural and functional studies of fucosylated or nonfucosylated glycoproteins is their structural microheterogeneity. Natural and recombinant fucosylated or nonfucosylated glycoproteins are typically produced as a mixture of glycoforms that differ only in the structure of the pendent oligosaccharides.

The remodeled glycoproteins, such as antibodies can be subjected to any further structural modifications that are necessary or desired, including, without limitation, glycosyl transfer, and selective ligation (e.g., click chemistry, Staudinger reaction, etc.) to introduce the additional functional groups or tags. The functional groups can be of any suitable type, including, without limitation, toxins, special antigens (such as alpha-Gal), radioactive species, photoactive species, PEGs, etc. The glycoprotein can be catalytically reacted in a “click chemistry” cycloaddition reaction of the azide functionality of the glycoprotein with an alkyne bearing the functional moiety of interest. The azido and alkyne functional groups can be switched in the respective ligation components, and the glycoprotein can be functionalized with an alkynyl functionality and reacted with an azide-functionalized compound including the moiety of interest. It will also be appreciated that other ligation pairs can be devised for the click chemistry reaction.

The core fucosylated and nonfucosylated antibodies or fragments thereof, produced according to the methods described herein, can be used for diagnosis and therapeutics. Approximately two-thirds of therapeutic proteins, such as monoclonal antibodies used on the market and/or currently in clinical trials are glycoproteins. However, the structural heterogeneity in different glycoforms of natural and recombinant glycoproteins presents a major barrier in developing glycoprotein-based drugs, as different glycoforms may have different biological activities and controlling glycosylation to a homogeneous glycoform is extremely difficult during expression. The previous discovery of the transglycosylation activity of a class of endoglycosidases represents a major advance in the field for glycosylation engineering to enhance glycoproteins' therapeutic and diagnostic potentials and the Endo-S mutants of the present invention are able to transglycosylate core fucosylated and nonfucosylated natural and recombinant glycoproteins without the negative aspects of hydrolysis.

The features and advantages of the present invention are more fully shown by the following non-limiting examples.

EXAMPLES

Saturation Site-Directed Mutagenesis of Endo-S at the Asp-233 Site

Previous mutational and structural studies have shown that the Asp-233 is a critical residue that promotes the formation of the sugar oxazolinium ion intermediate during enzymatic catalysis^(20, 27). In particular, two mutants have been identified, D233A and D233Q, that are glycosynthases capable of using glycan oxazoline as an activated glycosyl donor substrate for the glycosylation reaction with diminished hydrolysis activity on the product²⁰. In order to systematically screen for more efficient glycosynthase mutants of Endo-S, a library was constructed of Endo-S mutants by replacing the Asp-233 with the other 19 natural amino acids through saturation mutagenesis. The mutants were expressed and purified under the same conditions as for the wild-type Endo-S, and the yield of mutants (15-30 mg/L) were found to be comparable to that of the wild type Endo-S.

Comparison of Transglycosylation and Hydrolysis Activity of the Endo-S Mutants

The hydrolytic activity of the mutants generated was evaluated using rituximab as the substrate, and the transglycosylation activity was evaluated using the sugar oxazoline and the deglycosylated rituximab as the donor and acceptor substrates, respectively (Scheme 1). The results are summarized in Table 1. Comparison of the hydrolytic activity demonstrated that all 19 mutants, except for D233C, showed significantly diminished hydrolysis activity on the whole antibody in comparison with wild type Endo-S. Interestingly, the D233C (SEQ ID NO: 5) showed a similar hydrolysis activity as the wild-type Endo-S.

Among the mutants D233H, D233K, D233R, D233P, D233W and D233Y of SEQ ID NO: 1 showed less than 0.5% of the intrinsic hydrolytic activity of the wild-type Endo-S, whereas D233C still retained a significant capacity to hydrolyze the antibody Fc N-glycans at Asn-297. On the other hand, the transglycosylation assay revealed that most Endo-S mutants were able to transfer a biantennary complex-type glycan oxazoline to a deglycosylated rituximab antibody with varied efficiencies. In particular, D233C (SEQ ID NO: 5), D233E (SEQ ID NO: 6), D233G (SEQ ID NO: 7), D233M (SEQ ID NO: 2) and D233N (SEQ ID NO: 8) demonstrated the most significant transglycosylation activities, while the mutants D233F, D233I, and D233L of SEQ ID NO: 1 had only marginal transglycosylation activity. However, by comparing the overall transglycosylation efficiencies, most mutants with potent transglycosylation activities also possessed residual hydrolysis activity, a property less ideal for antibody glycosylation remodeling. For instance, D233C (SEQ ID NO: 5) showed the highest activity for both hydrolysis and transglycosylation among all the mutants, but its overall efficiency for glycoform synthesis (defined by the ratio of transglycosylation/hydrolysis, T/H) was only moderate. Interestingly, D233M (SEQ ID NO: 2) mutant demonstrated a relatively high transglycosylation activity among the mutants with a remarkably low residual hydrolysis activity. Thus, the highest overall synthetic efficiency makes D233M the most efficient glycosynthase mutant of Endo-S for antibody glycoengineering among the mutants. Based on the results of transglycosylation and residual hydrolysis activities of the mutants (Table 1), D233M showed an approximately 3- and 8-fold enhanced synthetic efficiency (T/H) over the previously reported Endo-S mutants, D233Q (SEQ ID NO: 3) and D233A (SEQ ID NO: 4), respectively²⁰. To demonstrate the improved catalytic efficiency of the Endo-S D233M mutant for the antibody Fc glycan remodeling, the transglycosylation reaction of the three selected mutants, D233M, D233Q and D233A was compared with the glycan oxazoline under the same glycosylation conditions. The parallel reactions were monitored by LC-ESI-MS (FIG. 1). The time-course of the glycosylation indicated that mutant D233M was more efficient than the previously identified mutants, D233A and D233Q²⁰.

Kinetic Analysis of Endo-S D233M and Endo-S D233A

The observed difference in the catalytic activity of D233M and D233A mutants was the impetus to perform a kinetic analysis of the two mutants. Using a sialylated glycan oxazoline (SCT-Oxa) as the donor and the deglycosylated rituximab as the acceptor substrate, we measured the kinetic parameters of the enzyme catalyzed glycosylation were measured. A mass spectrometry-based approach with an internal standard was used to estimate the product formation.³¹⁻³³. The results are summarized in Tables 2 and 3. For the biantennary complex-type glycan oxazoline (SCT-Oxa), the catalytic efficiency of Endo-S D233M (k_(cat)/K_(M)=0.03 min^(−1 μ)M⁻¹) showed a 3-fold increase in comparison with that of Endo-S D233A (k_(cat)/K_(M)=0.01 min⁻¹ μM⁻¹) (Table 2 and FIG. 2a ). The apparent increase in k_(cat)/K_(M) of Endo-S D233M over D233A was a result of approximately 4-fold increase in turnover (as measured by k_(cat)) and a less than 2-fold reduced affinity as estimated by the K_(M) value, as a higher K_(M) value is indicative of a lower substrate affinity. These results suggested that substitution with a methionine instead of an alanine at Asp-233 enhanced the enzymatic turnover number with a moderate decrease on the substrate affinity for the glycan oxazoline substrate.

TABLE 2 Kinetic parameters of Endo-S mutants Endo-S D233M and D233A for SCT-Oxa k_(cat) K_(M) k_(cat)/K_(M) Enzyme (min⁻¹) (μM) (min⁻¹ μM⁻¹) Endo-S D233M 4.99 ± 0.91 195.40 ± 7.21  0.03 Endo-S D233A 1.34 ± 0.19 87.91 ± 10.13 0.01

For the glycosyl acceptor substrate, the deglycosylated antibody, the Endo-S D233M mutant showed a much higher substrate affinity than the D233A mutant. This was clearly supported by the Michaelis-Menten curves of the two mutants (FIG. 2b ), which demonstrated that Endo-S D233M was much easier to saturate than the D233A mutant by the antibody substrate. The K_(M) of D233M for the deglycosylated antibody was 30 μM, while the K_(M) of D233A for the deglycosylated antibody was >200 μM (Table 3) On the other hand, the catalytic turnover number of Endo-S D233A (k_(cat)) for the antibody substrate could not be accurately measured because the concentration of the deglycosylated antibody required to saturate the enzyme was difficult to achieve.

TABLE 3 Kinetic parameters of Endo-S mutants Endo-S D233M and D233A for rituximab k_(cat) K_(M) k_(cat)/K_(M) Enzyme (min⁻¹) (μM) (min⁻¹ μM⁻¹) Endo-S D233M 5.53 ± 1.91 30.22 ± 7.21 0.18 Endo-S D233A —* >200 —* *The catalytic turnover number of Endo-S D233A could not be accurately determined by the software due to the fact that the concentration required for enzyme saturation exceeded the limits of the solubility of the deglycosylated antibody in solution.

Kinetic Analysis of Endo-S2 D184M and Endo-S2 D184A

Endo-S2 is another endoglycosidase from Streptococcus pyogenes serotype M49 that shows much broader substrate specificity than Endo-S for antibody degycosylation³⁰. A recent study on the mutations at the critical Asp-184 residue has identified the D184M mutant as the most efficient glycosynthase mutant within the systematic library of Endo-S2 variants generated through saturation mutagenesis²⁹. To evaluate the nature of the enhanced catalytic efficiency, the kinetic parameters of D184M and D184A mutants of wild type Endo-S2 (SEQ ID NO: 11) were also measured. The results revealed a similar pattern between the Endo-S and Endo-S2 mutants. For the sugar oxazoline substrate, the Endo-S2 methionine mutation significantly enhanced the catalytic efficiency (k_(cat)/K_(M)) in comparison with the alanine mutation, and a more than 10-fold increase in k_(cat)/K_(M) value was observed for the D184M mutant over the D184A mutant (Table 4 and FIG. 3a ). In analogy to Endo-S, the increased k_(cat)/K_(M) value for D184M mutant was caused by a more than 15-fold increase in catalytic turnover numbers (k_(cat)) and a less than 2-fold decrease in substrate affinity (K_(M)) for the glycan oxazoline substrate.

For the deglycosylated rituximab, like the Endo-S D233M mutant, the Endo-S2 D184M mutant also showed a significantly higher substrate affinity for the antibody than the Endo-S2 D184A mutant. The K_(M) value of Endo-S2 D184A was estimated to be more than 20 times higher than that of the Endo-S2 D184M. Similar to the case of Endo-S, Michaelis-Menten curves also indicated that the Endo-S2 D184A mutant showed no sign of saturation within the range of concentrations of antibody tested. Therefore, the catalytic turnover number of the Endo-S2 D184A also couldn't be accurately measured due to the difficulty to reach a saturated concentration of the substrate (Table 5 and FIG. 3b ).

Interestingly, for both the sugar oxazoline and the antibody substrates, Endo-S2 D184M demonstrated a significantly higher catalytic turnover number than Endo-S D233M, whereas the substrate affinity for both substrates proved to be comparable between the two mutants. Therefore, the overall catalytic efficiency (k_(cat)/K_(M)) of Endo-S2 D184M was found to be higher than that of Endo-S D233M.

TABLE 4 Kinetic parameters of Endo-S2 mutants D184M and D184A for SCT-Oxa k_(cat) k_(cat)/K_(M) Enzyme (min⁻¹) K_(M)(μM) (min⁻¹ μM⁻¹) Endo-S2 D184M 167.81 ± 20.50 229.10 ± 34.80 0.73 Endo-S2 D184A 10.20 ± 2.37 121.31 ± 17.14 0.08

TABLE 5 Kinetic parameters of Endo-S2 mutants D184M and D184A for rituximab k_(cat) k_(cat)/K_(M) Enzyme (min⁻¹) K_(M)(μM) (min⁻¹ μM⁻¹) Endo-S2 D184M 29.84 ± 9.30 32.62 ± 6.71 0.91 Endo-S2 D184A —* >680 —* *The catalytic turnover number of Endo-S D233A could not be accurately determined by the software due to the fact that the concentration required for enzyme saturation exceeded the limits of the solubility of the deglycosylated antibody in solution.

Discussion

Two glycosynthase mutants, D233A and D233Q of Endo-S have been previously identified, which could transfer glycan oxazoline to Fc-deglycosylated antibody to form homogeneous antibody glycoforms²⁰. More recently, new glycosynthase mutants from Endo-S2 have been identified by mutation at the critical Asp-184 residue, which show broader substrate specificity and distinct efficiency for antibody Fc glycan remodeling²⁹. However, a systematic mutagenesis on prototype enzyme Endo-S at the critical Asp-233 site had not been studied and the mechanism behind the observed difference in catalysis by different mutants remained to be characterized. In the present work, a systematic mutagenesis of Endo-S was performed by generating all the 19 natural amino acid mutants at the Asp-233 residue of Endo-S and examined their residual hydrolysis activity and transglycosylation activity. The present invention identified several novel glycosynthase mutants of Endo-S such as the D233M mutant that demonstrated enhanced transglycosylation activity with diminished hydrolysis of product. The kinetic analysis revealed that the enhanced catalytic efficiency of the Endo-S2 D184M mutant over the D184A mutant contributed mainly by two factors: the increased turnover for the glycan oxazoline donor substrate and the enhanced affinity for the antibody substrate. This is also true for the observed enhanced catalytic efficacy of the Endo-S D233M mutant over the Endo-S D233A mutant. It is still not clear how the methionine mutation leads to the increased turnover of the glycan oxazoline substrate and the enhanced affinity for the antibody substrate. The crystal structure of Endo-S enzyme and more recently the crystal structure of the Endo-S2 in complex with a complex type N-glycan were solved^(27, 28). But, unfortunately, the structure of the Endo-S2 or Endo-S complexed with an antibody Fc domain remains to be solved, which may provide an answer to the role of the methionine mutation at the critical D184 (for Endo-S2) or D233 (for Endo-S) residue in improving the glycosynthase activity.

Conclusion

It was found herein that in addition to the previously identified D233A and D233Q mutants of Endo-S, most of the Asp-233 mutants discovered here were also glycosynthases that demonstrated glycosylation activity using glycan oxazoline as the donor substrate with diminished hydrolysis activity. The glycosynthase activity of the resultant mutants varied significantly depending on the nature of the amino acid substituents. Among them, the D233M mutant was identified as the most efficient glycosynthase variant with the highest transglycosylation/hydrolysis ratio. Kinetic studies on the D233M and D233A mutants of Endo-S indicated that the enhanced catalytic efficacy of the Asp-to-Met mutant was mainly due to increased turnover (kcat) for the glycan oxazoline substrate and the significantly enhanced affinity (as judged by the reduced K_(M) value) for the antibody acceptor, respectively.

Methods and Material

Monoclonal antibody, rituximab, was purchased from Genentech Inc., (South San Francisco, Calif.). Sialoglycan complex-type oxazolines were chemically synthesized according to the previously published procedure³⁴. The wild-type Endo-S/S2 and mutants were expressed and purified according to protocols from our previous studies²⁰.

Site-Directed Mutagenesis, Expression and Purification of Recombinant Endo-S and Mutants

The pGEX plasmid vector encoding the wild-type Endo-S was a gift from Dr. M. Collin (Lund University, Sweden). The Endo-S mutants were generated using the Q5 Site-Directed Mutagenesis Kit (NEB) by the manufacturer's instructions. For systematic mutagenesis at Asp-233, two degenerate primers were used: 5′ CGTAAATTCGTGCTCAATNNNAATATCTAG TCCATCGACACCACGATCAGTT-3′ (forward) (SEQ ID NO: 9) and 5′-AACTGATCGTGGTGTCGATGGACTAGATATTNNNATTGAGCACGAATTTACG-3′ (SEQ ID NO: 10) (Reverse). Mutations were verified by DNA sequencing. The plasmid DNA encoding the wild type and mutant Endo-S genes was transformed in E. coli BL21 (DE3) cells for overexpression.

For simultaneous purification of all 20 Endo-S enzymes, the transformed cells were grown in 20 mL 2YT media with 100 μg/mL Carbenicillin added. Cells were incubated at 37° C. and induced with 0.5 mM isopropyl β-D-1-thiogalactopyranoside (IPTG) when they reached an OD600 of 0.8-1.0. The induced cells were incubated at 20° C. overnight and harvested by centrifugation. The cell lysates were collected after treating with bacterial cell lysis buffer (Gold Biotechnology, Inc.) following manufacturer's instructions. The GST-tagged proteins were purified using the GST Spin Column Kit (Thermo). The purified proteins were diluted into PBS at pH 7.4 after buffer exchange using Amicon ultra filtration units (10 kDa, Millipore). The purity of EndoS proteins was over 90% on SDS-PAGE and the final concentration was recorded on a NanoDrop 2000c at absorbance 280 nm. The expression and purification of Endo-S2 mutants were performed following our recent publication²⁰. Both enzymes and their mutants showed similar expression yield and purity (>90%).

Synthesis of the Fucα1,6GlcNAc-Rituximab Through the Wild-Type Endo-S Deglycosylation

In order to generate deglycosylated rituximab for transglycosylation assays, commercial antibody was treated with the wild-type Endo-S at a substrate-to-enzyme ratio of 1000:1 (w/w) for 30 min at 37° C. to release the heterogeneous N-glycoforms. Complete hydrolysis of glycans was confirmed by LC-MS analysis. The product GlcNAc-rituximab was subsequently purified through protein-A affinity chromatography. The deconvoluted mass (m/z) of purified antibody corresponds well to the calculated mass of Fucα1,6 GlcNAc-rituximab.

Liquid Chromatography Mass Spectrometry (LC-ESI-MS) Analysis of IgG Antibody

The LC-MS characterization of different antibody glycoforms was conducted on an Exactive Plus Orbitrap instrument (Thermo Scientific). The intact antibody sample was analyzed with a Waters XBridge™ BEH300 C4 column (3.5 μm, 2.1×50 mm). The program includes a 9 min linear gradient of 5-90% MeCN containing 0.1% formic acid at a flow rate of 0.4 mL/min. The original mass data were processed through deconvolution and integration through MagTran Software (Amgen).

Quantification Using an Internal Standard and Single-Point Normalization Factor

Peptide-N-Glycosidase F (PNGase F) treated rituximab was used as the internal standard due to its similarities to the deglycosylated and transferred product in terms of their molecular structures and ionization efficiencies. After PNGase F treatment, a mutation will be introduced into the amino acid sequence of rituximab so the product antibody will not interfere with the reaction via re-glycosylation³⁵. A standard product S2G2F-rituximab was synthesized following the previously reported procedure²⁹. ESI-MS spectra indicated that the starting material had been completely converted to the transglycosylation product. Serial dilutions containing a gradient of S2G2F-rituximab (0, 0.25, 0.5, 0.75, 1.0, 1.25 and 1.5 μM) were mixed with a stock solution containing 0.67 μM internal standard. These mixed sample solutions were quantified by selected ion monitoring (SIM) to calculate the single-point normalization factor³¹. The factor could then be used to calculate the relative amount of the final product N-glycoform for each reaction in the following experiments.

Transglycosylation and Hydrolysis Activity Assays

The hydrolytic activity of each Endo-S mutants and the wild-type (0.01 mg/mL) was assayed in PBS (pH 7.4, 10 μl) at 30° C. with synthetic biantennary sialo-complex-type rituximab (1.0 mg/mL, 6.9 μM) as the starting material. Each reaction was terminated at 5 min and an aliquot was taken from the reaction mixture and dissolved in 0.1% formic acid. The relative quantity of the hydrolysis product was calculated through deconvolution and integration of the selected MS peaks. The experimental details of product quantification using LC-MS are illustrated below. The transglycosylation activity of Endo-S was measured in a similar fashion: deglycosylated Rituximab (10.0 mg/mL, 69 μM) was incubated with SCT-Oxa (1.38 mM, 20 eq) under catalysis of Endo-S enzymes (0.01 mg/mL) under the same condition as hydrolysis. The transglycosylation product SCT-Rituximab was analyzed as mentioned above. Both functional assays were repeated twice for each mutant and the wild-type, and the average activity was recorded

Kinetic Measurements for the Endo-S and Endo-S2 Mutants

Measurements of K_(M) and Vmax for SCT-oxa. Serial dilutions with a total volume of 10 μL were prepared with a gradient of SCT-oxa concentrations and a constant deglycosylated antibody concentration mixed in PBS, pH 7.4. Each reaction was initiated by adding 1 μL of Endo-S/S2 mutants with a concentration of 0.1 mg/Ml and the reaction was conducted at 30° C. The concentrations of SCT-oxa were within a range from 6.25 μM to 400 μM. For each reaction, three aliquots were taken at t=1, 2 and 3 min and immediately quenched in 100 μL 0.1% formic acid. The quenched reaction samples were then characterized by ESI-MS, and the concentration of product in each mixture was calculated using the normalization factor, as shown above. A linear progression curve was confirmed for each reaction by sampling at multiple early time points and plotting them in the same graph, which emphasized that the V₀ measured indeed represents the initial rate of each reaction. The K_(M) and Vmax were measured by fitting the initial velocity against the SCT-oxa concentration using the GraphPad Prism7 program. The experiments were conducts in triplicate to determine the error in these measurements. A control reaction without the enzyme was set up for each reaction to confirm that non-enzymatic transfer of SCT-Oxa to the antibody did not happen and the results obtained here indeed represent the specific activity of each mutant.

Measurements of K_(M) and Vmax for the Deglycosylated Rituximab.

The K_(M) and Vmax values of both Endo-S and Endo-S2 mutants for the deglycosylated antibody substrate were measured in a similar fashion as to those for SCT-Oxa. In the serial reactions, the concentrations of antibody range from 0.313 μM to 20 μM, whereas the SCT-Oxa concentration was fixed at 400 μM. A similar control reaction was also performed for each concentration to monitor the non-enzymatic side reactions.

TABLE 1 Comparison of the specific transglycosylation efficiencies of the Endo-S D233 mutants measured by LC-ESI-MS using commercial rituximab as the substrate. The experiments were conducted in duplicate. Specific Hydrolysis Transglycosylation Transglycosylation/ Endo-S Activity Activity Hydrolysis Ratio Mutants 100*(μmol/min/mg) 100*(μmol/min/mg) T/H WT 2.77 25.89 9.35 D233A 0.06 1.06 17.67 D233C 0.92 21.29 23.14 D233E 0.36 9.45 26.25 D233F 0.02 0.16 8.00 D233G 0.25 3.13 12.52 D233H 0.01 0.00 0.00 D233K 0.01 0.00 0.00 D233R 0.01 0.00 0.00 D233I 0.04 0.14 3.50 D233L 0.02 0.14 7.00 D233M 0.02 2.71 135.50 D233N 0.43 2.96 6.88 D233P 0.02 0.00 0.00 D233Q 0.05 0.98 19.60 D233S 0.36 3.65 10.14 D233T 0.21 1.79 8.52 D233V 0.21 0.25 1.19 D233W 0.01 0.00 0.00 D233Y 0.01 0.26 26.00

The references cited herein are incorporated by reference herein for all purposes.

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That which is claimed is:
 1. A method of preparing a core fucosylated or nonfucosylated antibody or Fc fragment thereof having a predetermined oligosaccharide moiety, the method comprising: providing an antibody or Fc fragment comprising a core fucosylated or nonfucosylated GlcNAc-acceptor; and enzymatically reacting the core fucosylated or nonfucosylated GlcNAc-acceptor with an activated oligosaccharide donor using a Streptococcus pyogenes Endoglycosidase-S Asp233 mutant having an amino acid sequence comprising SEQ ID NO: 2 or mutants have at least 95% homology thereto, wherein the activated oligosaccharide donor carries an oligosaccharide moiety comprising a predetermined number and type of sugar residues, wherein via an enzymatic reaction, the activated oligosaccharide moiety is covalently linked to the core fucosylated or nonfucosylated GlcNAc-acceptor, thereby preparing the fucosylated or nonfucosylated antibody or Fc fragment having the predetermined oligosaccharide moiety.
 2. The method of claim 1, wherein the activated oligosaccharide component is a synthetic oligosaccharide oxazoline or sialylated oxazoline.
 3. The method of claim 1, wherein the synthetic oligosaccharide oxazoline is a di-, tri-, tetra-, penta-, hexyl-, hepta-, octyl-, nona-, deca- or undeca-saccharide oxazoline.
 4. The method of claim 1, wherein the activated oligosaccharide component further comprises an additional biologically active agent or a tag.
 5. The method of claim 4, wherein the additional biologically active agent or tag is a drug, toxin, fluorescent probe, biotin, a PEG, lipid, or polypeptide.
 6. The method of claim 1, wherein the fucosylated GlcNAc-acceptor is an alpha-1-6-fucosyl-GlcNAc-protein.
 7. The method of claim 1, wherein the core fucosylated or nonfucosylated antibody is a monoclonal antibody selected from the group consisting of 17b, 48d, A32, C11, 2G12, F240, IgG1b12, 19e, X5, TNX-355, cetuximab, rituximab, muromonab-CD3, abciximab, daclizumab, basiliximab, palivizumab, infliximab, trastuzumab, gemtuzumab ozogamicin, alemtuzumab, ibritumomab tiuxetan, adalimumab, omalizumab, tositumomab, 1-131 tositumomab, efalizumab, bevacizumab, panitumumab, pertuzumab, natalizumab, etanercept, IGN101, volociximab, Anti-CD80 mAb, Anti-CD23 mAb, CAT-3888, CDP-791, eraptuzumab, MDX-010, MDX-060, MDX-070, matuzumab, CP-675,206, CAL, SGN-30, zanolimumab, adecatumumab, oregovomab, nimotuzumab, ABT-874, denosumab, AM 108, AMG 714, fontolizumab, daclizumab, golimumab, CNTO 1275, ocrelizumab, HuMax-CD20, belimumab, epratuzumab, MLN1202, visilizumab, tocilizumab, ocrerlizumab, certolizumab pegol, eculizumab, pexelizumab, abciximab, ranibizimumab, mepolizumab and MYO-029.
 8. The method of claim 1, wherein the antibody further comprises an additional moiety selected from a group consisting of a therapeutic agent for treating cancer, a therapeutic agent for HIV, a toxin, an antibody different from the modified antibody which is reactive to another receptor, an antigen, a chemokine and a cytokine.
 9. A method of synthesizing a homogeneous core fucosylated or nonfucosylated IgG glycoprotein or IgG-Fc fragment, the method comprising: (a) providing a core fucosylated or nonfucosylated IgG glycoprotein or IgG-Fc fragment comprising heterogeneous or undesired N-glycans; (b) removing the heterogeneous or undesired N-glycans by an enzyme selected from the group Endo-H, Endo-F3, Endo S or Endo-A to form a core homogeneous fucosylated or nonfucosylated GlcNAc-IgG acceptor; (c) providing an oligosaccharide containing oxazoline with a desired oligosaccharide component comprising a N-glycan having a defined number and type of sugar residues; (d) enzymatically transglycosylating the core fucosylated or nonfucosylated GlcNAc-IgG acceptor with the oligosaccharide containing oxazoline using a Streptococcus pyogenes Endo-S Asp233 mutant comprising SEQ ID NO: 2 or mutants have at least 95% homology thereto, thereby forming homogeneous core fucosylated or nonfucosylated IgG glycoprotein or IgG-Fc fragment having the defined number and type of sugar residues.
 10. The method of claim 9, wherein the oligosaccharide containing oxazoline is a di-, tri-, tetra-, penta-, hexyl-, hepta-, octyl-, nona-, deca-, or undeca-saccharide oxazoline.
 11. The method of claim 9, wherein the core-fucosylated GlcNAc containing protein is an alpha-1-6-fucosyl-GlcNAc-protein.
 12. A method of synthesizing a modified antibody or Fc-fragment thereof, the method comprising; providing an antibody or Fc fragment comprising a fucosylated or nonfucosylated N-acetylglucosamine (GlcNAc) moiety to form a GlcNAc-protein acceptor; wherein the fucosylated or nonfucosylated N-acetylglucosamine (GlcNAc) moiety is positioned on the Fc region of the antibody; transglycosylating an oligosaccharide oxazoline having a predetermined number of saccharides and the GlcNAc-peptide acceptor under the catalysis of a Streptococcus pyogenes Endo-S Asp 233 mutant enzyme comprising SEQ ID NO: 2 or mutants have at least 95% homology thereto to form the modified antibody or Fc fragment with the predetermined number of saccharides.
 13. The method of claim 12 wherein the modified antibody further comprises an additional moiety including, a therapeutic agent for treating cancer, a therapeutic agent for HIV; a toxin, an antibody different from the modified antibody which is reactive to another receptor, an antigen, a therapeutic polypeptide, a chemokine and/or a cytokine attached to the oligosaccharide oxazoline.
 14. A delivery device for delivering a drug having biological activity to treat a condition, the delivery device comprising: a remodeled antibody comprising a recombinant fucosylated or nonfucosylated antibody having a predetermined number of sugar residues and a therapeutic agent attached to a terminal sugar or sialylated group, wherein the remodeled antibody is synthesized according to the method of claim
 9. 15. The delivery device of claim 14, wherein the remodel antibody is an antibody selected from the group consisting of 17b, 48d, A32, C11, 2G12, F240, IgG1b12, 19e, X5, TNX-355, cetuximab, rituximab, muromonab-CD3, abciximab, daclizumab, basiliximab, palivizumab, infliximab, trastuzumab, gemtuzumab ozogamicin, alemtuzumab, ibritumomab tiuxetan, adalimumab, omalizumab, tositumomab, I-131 tositumomab, efalizumab, bevacizumab, panitumumab, pertuzumab, natalizumab, etanercept, IGN101, volociximab, Anti-CD80 mAb, Anti-CD23 mAb, CAT-3888, CDP-791, eraptuzumab, MDX-010, MDX-060, MDX-070, matuzumab, CP-675,206, CAL, SGN-30, zanolimumab, adecatumumab, oregovomab, nimotuzumab, ABT-874, denosumab, AM 108, AMG 714, fontolizumab, daclizumab, golimumab, CNTO 1275, ocrelizumab, HuMax-CD20, belimumab, epratuzumab, MLN1202, visilizumab, tocilizumab, ocrerlizumab, certolizumab pegol, eculizumab, pexelizumab, abciximab, ranibizimumab, mepolizumab and MYO-029.
 16. The delivery device of claim 14, wherein the therapeutic agent is selected from an agent for treating cancer, a therapeutic agent for HIV, a toxin, an antibody different from the modified antibody which is reactive to another receptor, an antigen, a chemokine or a cytokine.
 17. A method of synthesizing intravenous immunoglobulin (WIG) preparation exhibiting Fc-sialylated glycoforms, the method comprising: providing an IVIG carrying Fc N-glycan; deglycosylating the Fc N-glycan using an endoglycosidase selected from the group Endo-H, Endo-F3, Endo S or Endo-A to form a GlcNAc-acceptor; wherein the GlcNAc-acceptor is positioned on the Fc region of the IVIG and the GlcNAc-acceptor is either core fucosylated or nonfucosylated; and transglycosylating the GlcNAc-acceptor on the IVIG with a sialoglycan oxazoline having a predetermined number of sugar residues under the catalysis of an enzyme selected from the group consisting of Endo-S mutants including SEQ ID NO: 2 to form a sialylated IVIG.
 19. A composition comprising a Streptococcus pyogenes Endo-S Asp-233 mutant comprising D233M (SEQ ID NO:2). 